id,agency_id,docket_id,title,document_type,subtype,posted_date,posted_year,posted_month,comment_start_date,comment_end_date,last_modified,fr_doc_num,open_for_comment,withdrawn,object_id
FDA-2021-N-0600-0001,FDA,FDA-2021-N-0600,Medical Devices; Cardiovascular Devices; Classification of the Intravascular Bleed Monitor,Rule,Final Rule,2022-06-08T04:00:00Z,2022,6,2022-06-08T04:00:00Z,,2022-06-08T13:55:34Z,2022-12364,0,0,090000648514d1b2